Wallner Stefan, Schröder Christopher, Leitão Elsa, Berulava Tea, Haak Claudia, Beißer Daniela, Rahmann Sven, Richter Andreas S, Manke Thomas, Bönisch Ulrike, Arrigoni Laura, Fröhler Sebastian, Klironomos Filippos, Chen Wei, Rajewsky Nikolaus, Müller Fabian, Ebert Peter, Lengauer Thomas, Barann Matthias, Rosenstiel Philip, Gasparoni Gilles, Nordström Karl, Walter Jörn, Brors Benedikt, Zipprich Gideon, Felder Bärbel, Klein-Hitpass Ludger, Attenberger Corinna, Schmitz Gerd, Horsthemke Bernhard
Institute for Clinical Chemistry and Laboratory Medicine, University Hospital Regensburg, Regensburg, Germany.
Genome Informatics, Institute of Human Genetics, University Duisburg-Essen, Essen, Germany.
Epigenetics Chromatin. 2016 Jul 29;9:33. doi: 10.1186/s13072-016-0079-z. eCollection 2016.
Monocyte-to-macrophage differentiation involves major biochemical and structural changes. In order to elucidate the role of gene regulatory changes during this process, we used high-throughput sequencing to analyze the complete transcriptome and epigenome of human monocytes that were differentiated in vitro by addition of colony-stimulating factor 1 in serum-free medium.
Numerous mRNAs and miRNAs were significantly up- or down-regulated. More than 100 discrete DNA regions, most often far away from transcription start sites, were rapidly demethylated by the ten eleven translocation enzymes, became nucleosome-free and gained histone marks indicative of active enhancers. These regions were unique for macrophages and associated with genes involved in the regulation of the actin cytoskeleton, phagocytosis and innate immune response.
In summary, we have discovered a phagocytic gene network that is repressed by DNA methylation in monocytes and rapidly de-repressed after the onset of macrophage differentiation.
单核细胞向巨噬细胞的分化涉及主要的生化和结构变化。为了阐明这一过程中基因调控变化的作用,我们使用高通量测序分析了在无血清培养基中添加集落刺激因子1体外分化的人单核细胞的完整转录组和表观基因组。
大量的mRNA和miRNA显著上调或下调。超过100个离散的DNA区域,大多远离转录起始位点,被十一易位酶迅速去甲基化,成为无核小体状态,并获得了指示活性增强子的组蛋白标记。这些区域是巨噬细胞特有的,并且与参与肌动蛋白细胞骨架调节、吞噬作用和先天免疫反应的基因相关。
总之,我们发现了一个吞噬基因网络,该网络在单核细胞中被DNA甲基化抑制,并在巨噬细胞分化开始后迅速去抑制。